ENST00000342992.11:c.47743C>T
(TTN)
|
ENSP00000343764.6:p.Pro15915Ser
|
|
ENST00000342175.11:c.28828C>T
(TTN)
|
ENSP00000340554.6:p.Pro9610Ser
|
|
ENST00000359218.10:c.28627C>T
(TTN)
|
ENSP00000352154.5:p.Pro9543Ser
|
|
ENST00000342175.10:c.28828C>T
(TTN)
|
ENSP00000340554.6:p.Pro9610Ser
|
|
ENST00000342992.10:c.47743C>T
(TTN)
|
ENSP00000343764.6:p.Pro15915Ser
|
|
ENST00000359218.9:c.28627C>T
(TTN)
|
ENSP00000352154.5:p.Pro9543Ser
|
|
ENST00000460472.6:c.28252C>T
(TTN)
|
ENSP00000434586.1:p.Pro9418Ser
|
|
ENST00000589042.5:c.55447C>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Pro18483Ser
|
|
ENST00000591111.5:c.50524C>T
(TTN)
|
ENSP00000465570.1:p.Pro16842Ser
|
|
ENST00000615779.4:c.50524C>T
(TTN)
|
ENSP00000483597.1:p.Pro16842Ser
|
|
NM_001256850.1:c.50524C>T
(TTN)
|
NP_001243779.1:p.Pro16842Ser
|
|
NM_001267550.2:c.55447C>T
(TTN)
MANE Select
|
NP_001254479.2:p.Pro18483Ser
|
|
NM_003319.4:c.28252C>T
(TTN)
|
NP_003310.4:p.Pro9418Ser
|
|
NM_133378.4:c.47743C>T
(TTN)
|
NP_596869.4:p.Pro15915Ser
|
|
NM_133432.3:c.28627C>T
(TTN)
|
NP_597676.3:p.Pro9543Ser
|
|
NM_133437.4:c.28828C>T
(TTN)
|
NP_597681.4:p.Pro9610Ser
|
|
NR_038271.1:n.682+3869G>A
(TTN-AS1)
|
|
|
NR_038272.1:n.3917+883G>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.54544C>T
(TTN)
|
XP_011510031.1:p.Pro18182Ser
|
|
XM_011511730.1:c.28438C>T
(TTN)
|
XP_011510032.1:p.Pro9480Ser
|
|
XM_011511731.1:c.28297C>T
(TTN)
|
XP_011510033.1:p.Pro9433Ser
|
|
XM_017004819.1:c.54340C>T
(TTN)
|
XP_016860308.1:p.Pro18114Ser
|
|
XM_017004820.1:c.49738C>T
(TTN)
|
XP_016860309.1:p.Pro16580Ser
|
|
XM_017004821.1:c.49735C>T
(TTN)
|
XP_016860310.1:p.Pro16579Ser
|
|
XM_017004822.1:c.46777C>T
(TTN)
|
XP_016860311.1:p.Pro15593Ser
|
|
XM_017004823.1:c.28393C>T
(TTN)
|
XP_016860312.1:p.Pro9465Ser
|
|
XM_024453094.1:c.49888C>T
(TTN)
|
XP_024308862.1:p.Pro16630Ser
|
|
XM_024453095.1:c.49885C>T
(TTN)
|
XP_024308863.1:p.Pro16629Ser
|
|
XM_024453096.1:c.49318C>T
(TTN)
|
XP_024308864.1:p.Pro16440Ser
|
|
XM_024453097.1:c.46660C>T
(TTN)
|
XP_024308865.1:p.Pro15554Ser
|
|
XM_024453098.1:c.46579C>T
(TTN)
|
XP_024308866.1:p.Pro15527Ser
|
|
XM_024453099.1:c.28342C>T
(TTN)
|
XP_024308867.1:p.Pro9448Ser
|
|
XM_024453100.1:c.18196C>T
(TTN)
|
XP_024308868.1:p.Pro6066Ser
|
|